1416916-78-3

Basic information

• Product Name: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide
• Synonyms: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide
• CAS NO: 1416916-78-3
• Molecular Weight: 395.607
• Mol File: 1416916-78-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide(1416916-78-3)
• EPA Substance Registry System: 3,5-di-tert-butyl-N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide(1416916-78-3)

Safety Data

• Hazardous Substances Data: 1416916-78-3(Hazardous Substances Data)

Upstream product

• 73604-46-3 2,2-dimethyl-1-amino-pent-4-ene 
• 160252-94-8 3,5-di-tert-butyl-4-methoxybenzene-1-sulfonyl chloride 

Downstream Products

• 1416916-85-2 (S)-1-(1-((3,5-di-tert-butyl-4-methoxyphenyl)sulfonyl)-4,4-dimethylpyrrolidin-2-yl)methanol 
• 1416916-82-9 (S)-1-((1-((3,5-di-tert-butyl-4-methoxyphenyl)sulfonyl)-4,4-dimethylpyrrolidin-2-yl)methoxy)-2,2,6,6-tetramethylpiperidine 

Relevant articles and documents

Mechanistic analysis and optimization of the copper-catalyzed enantioselective intramolecular alkene aminooxygenation

The catalytic asymmetric aminooxygenation of alkenes provides an efficient and straightforward approach to prepare chiral vicinal amino alcohols. We have reported a copper(II)-catalyzed enantioselective intramolecular alkene aminooxygenation, using (2,2,6